Process Engineer - Purification & Separation Engineering, PS&E
Full-TimeUpdated on 10/23/2026
No salary listed
Junior
Bachelor's, Master's
Juncos, Puerto Rico
In PersonOn-site in Juncos, Puerto Rico.
Biology & BiotechBioprocess & Biomanufacturing
About the job
Requirements
A Master's degree in Engineering, or a Bachelor's degree in Engineering with at least 2 years of engineering experience.
Working knowledge of pharmaceutical or biotechnology processes is preferred.
Ability to operate specialized laboratory equipment and relevant software is preferred.
Understanding and application of Good Laboratory Practices and Good Manufacturing Practices is preferred.
Experience in purification operations is preferred.
Strong knowledge of chromatography and ultrafiltration/diafiltration techniques is preferred.
Technical report writing proficiency is preferred.
Personal organization, validation protocol, change management, equipment-specific technical knowledge, analytical problem solving, and computer literacy are preferred.
Responsibilities
Provide solutions to technical problems of moderate scope and complexity.
Evaluate, select, and apply standard engineering techniques and procedures, seeking guidance for unusual or complex issues.
Perform assignments with clear objectives that require investigating a limited number of variables.
Initiate and complete routine technical tasks independently.
Serve as a technical expert for equipment and systems during troubleshooting activities.
Engage directly in daily operations when needed to meet production schedules or resolve complex issues.
Conduct routine audits of equipment performance and regulatory compliance for systems of significant complexity.
Collaborate with cross-functional teams in Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, and Validation to define requirements and recommendations for system or process modifications.
Support project managers in completing design, engineering, and construction projects within established timelines and budgets.
Partner with consultants, architects, and engineering firms to develop standard design documentation.
Obtain and evaluate quotes for equipment modifications or installations.
Prepare basic project cost estimates and schedules.
Perform additional engineering duties as assigned.
Desired Qualifications
Working knowledge of pharmaceutical or biotechnology processes.
Ability to operate specialized laboratory equipment and relevant software.
Understanding and application of Good Laboratory Practices and Good Manufacturing Practices.
Experience in purification operations.
Strong knowledge of chromatography and ultrafiltration/diafiltration techniques.
Technical report writing proficiency.
Personal organization, validation protocol, change management, equipment-specific technical knowledge, analytical problem solving, and computer literacy.
Process Engineer - Purification & Separation Engineering (PS&E)
BioPharma Consulting JAD Group · Juncos, Puerto Rico · Contract · Posted 2026-09-19
Workplace: on_site
Description
Under general supervision, this role provides engineering support across operations, manufacturing, pilot plant, and capital project environments. Responsibilities include process optimization, troubleshooting operational issues, and applying engineering principles to system modifications, experiments, and small‑scope projects. The role requires strong analytical skills to organize, interpret, and present results for operational or engineering activities.
Responsibilities
Provide solutions to technical problems of moderate scope and complexity.
Evaluate, select, and apply standard engineering techniques and procedures; seek guidance for unusual or complex issues.
Perform assignments with clear objectives requiring investigation of a limited number of variables.
Initiate and complete routine technical tasks independently.
Serve as a technical expert for equipment and systems during troubleshooting activities.
Engage directly in daily operations when needed to meet production schedules or resolve complex issues.
Conduct routine audits of equipment performance and regulatory compliance for systems of significant complexity.
Collaborate with cross‑functional teams (Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, Validation) to define requirements and recommendations for system or process modifications.
Support project managers in completing design, engineering, and construction projects within established timelines and budgets.
Partner with consultants, architects, and engineering firms to develop standard design documentation.
Obtain and evaluate quotes for equipment modifications or installations.
Prepare basic project cost estimates and schedules.
Perform additional engineering duties as assigned.
Requirements
Master’s degree in Engineering OR
Bachelor’s degree in Engineering + 2 years of engineering experience
Preferred Qualifications
Working knowledge of pharmaceutical/biotech processes.
Ability to operate specialized laboratory equipment and relevant software.
Understanding and application of GLPs and GMPs.
Experience in purification operations.
Strong knowledge of chromatography and UFDF (Ultrafiltration/Diafiltration) techniques.
Technical report writing proficiency.
Solid understanding of validation protocol execution.